72162-1081 NDC - HYDROMORPHONE HYDROCHLORIDE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	72162-1081-0	10 TABLET in 1 BOTTLE, PLASTIC (72162-1081-0)	EA
2	72162-1081-3	30 TABLET in 1 BOTTLE, PLASTIC (72162-1081-3)	EA
3	72162-1081-6	60 TABLET in 1 BOTTLE, PLASTIC (72162-1081-6)	EA

Field Name	Field Value	Definition
PRODUCT NDC	72162-1081	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Hydromorphone Hydrochloride	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	12/9/2009	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
END MARKETING DATE	1/31/2022	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAME	ANDA	The translation of the dosage form Code submitted by the firm.
APPLICATION NUMBER	ANDA077471	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	Bryant Ranch Prepack	This is the date that the labeler indicates was the start of its marketing of the drug product.